Canonical Allele Identifier: CA1465794034
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670122T= , CM000666.2:g.68670122T= GRCh38
NC_000004.11:g.69535840T= , CM000666.1:g.69535840T= GRCh37
NC_000004.10:g.69218435T= NCBI36
NG_052676.1:g.5655A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.497A= MANE Select ENSP00000341045.5:p.Asn166=
ENST00000338206.5:c.497A= ENSP00000341045.5:p.Asn166=
ENST00000616841.4:c.497A= ENSP00000482004.1:p.Asn166=
NM_001076.3:c.497A= NP_001067.2:p.Asn166=
NM_001076.4:c.497A= MANE Select NP_001067.2:p.Asn166=
Search 100 bp 5'
Search 100 bp 3'